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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6891851copy number variation1nstd229human GRCh38 chr10: 103,994,859-104,941,952 , GRCh37.p13 chr10: 105,754,617-106,701,710 LOC105378464, GSTO1, 16 more genes
    nsv6891746copy number variation1nstd229human GRCh38 chr10: 104,079,778-104,153,317 , GRCh37.p13 chr10: 105,839,536-105,913,075 SFR1, CFAP43, 1 more genes
    nsv6884311copy number variation1nstd229human GRCh38 chr10: 104,100,632-104,131,671 , GRCh37.p13 chr10: 105,860,390-105,891,429 CFAP43, SFR1
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6637523copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,015,345-105,911,204 , GRCh38.p12 chr10: 103,255,588-104,151,446 PCGF6, INA, 20 more genes
    nsv6450059copy number variation1nstd223human GRCh38 chr10: 104,117,901-104,125,400 , GRCh37.p13 chr10: 105,877,659-105,885,158 SFR1
    nsv6131928copy number variation1nstd213human GRCh37 chr10: 105,830,000-106,160,001 , GRCh38.p12 chr10: 104,070,242-104,400,243 COL17A1, GSTO1, 10 more genes
    nsv4728834copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,839,235-105,890,455 , GRCh38.p12 chr10: 104,079,477-104,130,697 CFAP43, SFR1, 1 more genes
    nsv4605011copy number variation1nstd183human GRCh37 chr10: 105,881,710-105,891,455 , GRCh38.p12 chr10: 104,121,952-104,131,697 CFAP43, SFR1
    nsv4599751copy number variation1nstd183human GRCh37 chr10: 105,881,698-105,883,474 , GRCh38.p12 chr10: 104,121,940-104,123,716 SFR1
    nsv4527651copy number variation1nstd166human GRCh37.p13 chr10: 105,880,247-105,880,866 , GRCh38.p12 chr10: 104,120,489-104,121,108 SFR1
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 DPCD, LOC105378467, 504 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082 MIR4295, BORCS7, 508 more genes
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